Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: A newly recognized type of osteogenesis imperfecta-Reference-Cited by-同舟云学术

Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: A newly recognized type of osteogenesis imperfecta

Published:1987-01 Issue:1 Volume:110 Page:76-80
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

David Cole E.C.,Carpenter Thomas O.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference10 articles.

1. The brittle bone syndrome: osteogenesis imperfecta;Smith,1983

2. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J Med Genet,1979

3. Osteogenesis imperfecta: an expanding panorama of variants;Sillence;Clin Orthoped Rel Res,1981

4. Osteogenesis imperfecta: update and perspective;Byers;Am J Med Genet,1984

5. Heritable diseases of collagen;Prockop;N Engl J Med,1984

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